SV2A (synaptic vesicle glycoprotein 2A) - Rat Genome Database

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Gene: SV2A (synaptic vesicle glycoprotein 2A) Homo sapiens
Analyze
Symbol: SV2A
Name: synaptic vesicle glycoprotein 2A
RGD ID: 1604842
HGNC Page HGNC
Description: Predicted to enable protein kinase binding activity. Predicted to be involved in regulation of gamma-aminobutyric acid secretion; synaptic vesicle priming; and transmembrane transport. Predicted to act upstream of or within cellular calcium ion homeostasis. Located in endoplasmic reticulum.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: KIAA0736; SV2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1149,903,318 - 149,917,844 (-)EnsemblGRCh38hg38GRCh38
GRCh381149,903,318 - 149,917,844 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371149,874,870 - 149,889,396 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361148,141,859 - 148,156,054 (-)NCBINCBI36hg18NCBI36
Celera1122,990,840 - 123,005,404 (-)NCBI
Cytogenetic Map1q21.2NCBI
HuRef1121,255,354 - 121,269,918 (-)NCBIHuRef
CHM1_11151,271,444 - 151,286,008 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:1519064   PMID:7681585   PMID:9872452   PMID:10611374   PMID:10617638   PMID:11076863   PMID:11230166   PMID:11256614   PMID:12477932   PMID:15210974   PMID:15217342   PMID:15342556  
PMID:15489334   PMID:15489336   PMID:15822905   PMID:16303743   PMID:16344560   PMID:16381901   PMID:16710414   PMID:18029348   PMID:18391951   PMID:18524768   PMID:18977120   PMID:19220410  
PMID:19399787   PMID:20167814   PMID:21795655   PMID:21873635   PMID:21936812   PMID:23017826   PMID:23244111   PMID:23275563   PMID:23530581   PMID:23617838   PMID:23798571   PMID:24284412  
PMID:25326386   PMID:25429064   PMID:25692762   PMID:25921289   PMID:26186194   PMID:26241848   PMID:26339411   PMID:26639968   PMID:28298427   PMID:28514442   PMID:29180619   PMID:29997244  
PMID:31168673   PMID:31280863   PMID:31317476   PMID:31753913   PMID:32400950   PMID:32807901   PMID:32944949   PMID:34079125  


Genomics

Comparative Map Data
SV2A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1149,903,318 - 149,917,844 (-)EnsemblGRCh38hg38GRCh38
GRCh381149,903,318 - 149,917,844 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371149,874,870 - 149,889,396 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361148,141,859 - 148,156,054 (-)NCBINCBI36hg18NCBI36
Celera1122,990,840 - 123,005,404 (-)NCBI
Cytogenetic Map1q21.2NCBI
HuRef1121,255,354 - 121,269,918 (-)NCBIHuRef
CHM1_11151,271,444 - 151,286,008 (-)NCBICHM1_1
Sv2a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39396,088,543 - 96,102,499 (+)NCBIGRCm39mm39
GRCm39 Ensembl396,088,467 - 96,102,837 (+)Ensembl
GRCm38396,181,227 - 96,195,183 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl396,181,151 - 96,195,521 (+)EnsemblGRCm38mm10GRCm38
MGSCv37395,985,150 - 95,999,106 (+)NCBIGRCm37mm9NCBIm37
MGSCv36396,266,632 - 96,280,588 (+)NCBImm8
Celera397,620,657 - 97,631,186 (+)NCBICelera
Cytogenetic Map3F2.1NCBI
Sv2a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22183,741,455 - 183,757,290 (+)NCBI
Rnor_6.0 Ensembl2198,321,142 - 198,336,913 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.02198,321,100 - 198,336,889 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02217,808,165 - 217,823,872 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42190,989,187 - 191,000,859 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.12190,948,188 - 190,963,566 (+)NCBI
Celera2176,272,713 - 176,284,621 (+)NCBICelera
Cytogenetic Map2q34NCBI
Sv2a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955413834,743 - 851,023 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955413834,743 - 849,176 (+)NCBIChiLan1.0ChiLan1.0
SV2A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11128,904,140 - 128,918,829 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1128,904,151 - 128,918,829 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01125,247,429 - 125,262,041 (-)NCBIMhudiblu_PPA_v0panPan3
SV2A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11759,185,715 - 59,195,888 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1759,187,244 - 59,195,888 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1758,633,794 - 58,647,878 (-)NCBI
ROS_Cfam_1.01760,182,727 - 60,196,808 (-)NCBI
UMICH_Zoey_3.11759,032,197 - 59,046,284 (-)NCBI
UNSW_CanFamBas_1.01759,115,941 - 59,130,018 (-)NCBI
UU_Cfam_GSD_1.01759,843,004 - 59,857,105 (-)NCBI
Sv2a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505821,213,447 - 21,227,353 (-)NCBI
SpeTri2.0NW_004936580243,829 - 257,708 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SV2A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl499,138,342 - 99,153,149 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1499,138,319 - 99,153,153 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24108,567,034 - 108,581,274 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SV2A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Vero_WHO_p1.0NW_02366603813,389,665 - 13,404,056 (+)NCBI
Sv2a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462477217,684,061 - 17,698,728 (-)NCBI

Position Markers
D1S2222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371149,887,407 - 149,887,552UniSTSGRCh37
Build 361148,154,031 - 148,154,176RGDNCBI36
Celera1123,003,377 - 123,003,522RGD
Cytogenetic Map1q21.2UniSTS
HuRef1121,267,891 - 121,268,036UniSTS
Marshfield Genetic Map1161.05UniSTS
Marshfield Genetic Map1161.05RGD
A002I04  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371149,875,264 - 149,875,376UniSTSGRCh37
Build 361148,141,888 - 148,142,000RGDNCBI36
Celera1122,991,234 - 122,991,346RGD
Cytogenetic Map1q21.2UniSTS
HuRef1121,255,748 - 121,255,860UniSTS
GeneMap99-GB4 RH Map1538.16UniSTS
GeneMap99-GB4 RH Map1551.93UniSTS
Whitehead-RH Map1641.3UniSTS
NCBI RH Map11040.0UniSTS
RH12850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371149,874,998 - 149,875,139UniSTSGRCh37
Build 361148,141,622 - 148,141,763RGDNCBI36
Celera1122,990,968 - 122,991,109RGD
Cytogenetic Map1q21.2UniSTS
HuRef1121,255,482 - 121,255,623UniSTS
GeneMap99-GB4 RH Map1552.71UniSTS
NCBI RH Map1970.1UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2086
Count of miRNA genes:764
Interacting mature miRNAs:907
Transcripts:ENST00000369145, ENST00000369146
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 426 1100 434 11 210 11 784 265 2964 45 430 212 4 1 2 529
Low 1923 1104 1011 336 1191 175 2895 1065 769 326 1002 1349 169 1095 1685 4 2
Below cutoff 86 786 280 276 544 278 678 865 1 47 28 51 1 107 574 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_050966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001328674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001328675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC239868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL591493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC045111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP214143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ819355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA334809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC305069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000369145   ⟹   ENSP00000358141
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1149,905,472 - 149,917,841 (-)Ensembl
RefSeq Acc Id: ENST00000369146   ⟹   ENSP00000358142
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1149,903,318 - 149,917,844 (-)Ensembl
RefSeq Acc Id: NM_001278719   ⟹   NP_001265648
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381149,903,318 - 149,906,991 (-)NCBI
GRCh371149,874,870 - 149,889,434 (-)NCBI
HuRef1121,255,354 - 121,269,918 (-)NCBI
CHM1_11151,271,444 - 151,275,117 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001328674   ⟹   NP_001315603
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381149,903,318 - 149,917,844 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001328675   ⟹   NP_001315604
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381149,903,318 - 149,917,844 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014849   ⟹   NP_055664
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381149,903,318 - 149,917,844 (-)NCBI
GRCh371149,874,870 - 149,889,434 (-)ENTREZGENE
Build 361148,141,859 - 148,156,054 (-)NCBI Archive
HuRef1121,255,354 - 121,269,918 (-)ENTREZGENE
CHM1_11151,271,444 - 151,286,008 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_055664   ⟸   NM_014849
- Peptide Label: isoform 1
- UniProtKB: Q7L0J3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001265648   ⟸   NM_001278719
- Peptide Label: isoform 2
- UniProtKB: Q7L0J3 (UniProtKB/Swiss-Prot),   B4E000 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001315604   ⟸   NM_001328675
- Peptide Label: isoform 1
- UniProtKB: Q7L0J3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001315603   ⟸   NM_001328674
- Peptide Label: isoform 1
- UniProtKB: Q7L0J3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000358141   ⟸   ENST00000369145
RefSeq Acc Id: ENSP00000358142   ⟸   ENST00000369146
Protein Domains
MFS

Promoters
RGD ID:6856926
Promoter ID:EPDNEW_H1628
Type:initiation region
Name:SV2A_1
Description:synaptic vesicle glycoprotein 2A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381149,917,842 - 149,917,902EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_014849.4(SV2A):c.1740G>A (p.Lys580=) single nucleotide variant Malignant melanoma [RCV000064121] Chr1:149906795 [GRCh38]
Chr1:149878347 [GRCh37]
Chr1:148144971 [NCBI36]
Chr1:1q21.2
not provided
NM_014849.5(SV2A):c.1148G>A (p.Arg383Gln) single nucleotide variant Inborn genetic diseases [RCV000190816] Chr1:149909832 [GRCh38]
Chr1:149881384 [GRCh37]
Chr1:1q21.2
uncertain significance
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
GRCh37/hg19 1q21.2(chr1:149783688-150049029)x3 copy number gain Ductal breast carcinoma [RCV000207055] Chr1:149783688..150049029 [GRCh37]
Chr1:1q21.2
uncertain significance
GRCh37/hg19 1q21.1-21.3(chr1:144927578-153223600)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV000223957] Chr1:144927578..153223600 [GRCh37]
Chr1:1q21.1-21.3
pathogenic
GRCh37/hg19 1q21.1-21.3(chr1:143753740-151399970)x3 copy number gain See cases [RCV000447109] Chr1:143753740..151399970 [GRCh37]
Chr1:1q21.1-21.3
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q21.2(chr1:149802401-149944241)x3 copy number gain not provided [RCV000684654] Chr1:149802401..149944241 [GRCh37]
Chr1:1q21.2
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_014849.5(SV2A):c.1674C>T (p.Asn558=) single nucleotide variant not provided [RCV000979991] Chr1:149907704 [GRCh38]
Chr1:149879256 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.918C>T (p.Tyr306=) single nucleotide variant not provided [RCV000948558] Chr1:149910863 [GRCh38]
Chr1:149882415 [GRCh37]
Chr1:1q21.2
benign
NM_014849.5(SV2A):c.417A>G (p.Ala139=) single nucleotide variant not provided [RCV000915270] Chr1:149913424 [GRCh38]
Chr1:149884976 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.564C>T (p.Phe188=) single nucleotide variant not provided [RCV000883587] Chr1:149913277 [GRCh38]
Chr1:149884829 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.1773C>T (p.Gly591=) single nucleotide variant not provided [RCV000916470] Chr1:149906762 [GRCh38]
Chr1:149878314 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.1941T>C (p.Ser647=) single nucleotide variant not provided [RCV000895955] Chr1:149905984 [GRCh38]
Chr1:149877536 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.2121C>T (p.Phe707=) single nucleotide variant not provided [RCV000961302] Chr1:149905122 [GRCh38]
Chr1:149876674 [GRCh37]
Chr1:1q21.2
benign
NM_014849.5(SV2A):c.1758C>T (p.Asp586=) single nucleotide variant not provided [RCV000958485] Chr1:149906777 [GRCh38]
Chr1:149878329 [GRCh37]
Chr1:1q21.2
benign
NM_014849.5(SV2A):c.1338C>T (p.Ile446=) single nucleotide variant not provided [RCV000974595] Chr1:149909233 [GRCh38]
Chr1:149880785 [GRCh37]
Chr1:1q21.2
benign
NM_014849.5(SV2A):c.117C>T (p.Asp39=) single nucleotide variant not provided [RCV000930470] Chr1:149913724 [GRCh38]
Chr1:149885276 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.2148C>A (p.Ile716=) single nucleotide variant not provided [RCV000908468] Chr1:149905095 [GRCh38]
Chr1:149876647 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.200GAG[1] (p.Gly68del) microsatellite not provided [RCV000894249] Chr1:149913636..149913638 [GRCh38]
Chr1:149885188..149885190 [GRCh37]
Chr1:1q21.2
likely benign
NM_014849.5(SV2A):c.2109C>T (p.Ile703=) single nucleotide variant not provided [RCV000955774] Chr1:149905134 [GRCh38]
Chr1:149876686 [GRCh37]
Chr1:1q21.2
benign
NM_014849.5(SV2A):c.1083C>T (p.Phe361=) single nucleotide variant not provided [RCV000890878] Chr1:149910576 [GRCh38]
Chr1:149882128 [GRCh37]
Chr1:1q21.2
benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20566 AgrOrtholog
COSMIC SV2A COSMIC
Ensembl Genes ENSG00000159164 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000358141 UniProtKB/Swiss-Prot
  ENSP00000358142 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000369145 UniProtKB/Swiss-Prot
  ENST00000369146 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000159164 GTEx
HGNC ID HGNC:20566 ENTREZGENE
Human Proteome Map SV2A Human Proteome Map
InterPro MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_sugar_transport-like UniProtKB/Swiss-Prot
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sugar_transporter_CS UniProtKB/Swiss-Prot
  SV2 UniProtKB/Swiss-Prot
KEGG Report hsa:9900 UniProtKB/Swiss-Prot
NCBI Gene 9900 ENTREZGENE
OMIM 185860 OMIM
Pfam MFS_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sugar_tr UniProtKB/Swiss-Prot
PharmGKB PA128394564 PharmGKB
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
TIGRFAMs synapt_SV2 UniProtKB/Swiss-Prot
UniProt B4E000 ENTREZGENE, UniProtKB/TrEMBL
  L8E840_HUMAN UniProtKB/TrEMBL
  Q7L0J3 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DUZ7 UniProtKB/Swiss-Prot
  O94841 UniProtKB/Swiss-Prot
  Q5QNX8 UniProtKB/Swiss-Prot
  Q7Z3L6 UniProtKB/Swiss-Prot
  Q8NBJ6 UniProtKB/Swiss-Prot
  Q9BVZ9 UniProtKB/Swiss-Prot